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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1112015생성일: 2026년 10월 26일

2-(Cyclohexylthio)-1H-isoindole-1,3(2H)-dione → Phthalimide

https://huagongshe.com/reaction/1112015

반응식

참여 물질

역할이름HCID투입량
반응물2-(Cyclohexylthio)-1H-isoindole-1,3(2H)-dioneHCID 28777—
용매HeptaneHCID 8900—
생성물PhthalimideHCID 6809—

반응 단계

13.1 Grams (0.05 mole) of N-(cyclohexylthio)phthalimide and 6.9 grams (0.05 mole) of benzoyl thiol(thiobenzoic acid) in 150 ml of heptane are stirred overnight at room temperature. The precipitate is recovered by filtration, washed with carbon tetrachloride and dried. 7.3 Grams of phthalimide (m.p. 234° C.) are obtained. The solvent is removed from the filtrate by evaporation under reduced pressure. 12 Grams (95% yield) of product, a light brown liquid, are obtained. The identity of the benzoylcyclohexyl disulfide is confirmed by GLC and NMR analyses. Analysis gives 25.51% sulfur compared to 25.45% sulfur calculated for C13H16OS2. Similarly, except N-(2-benzothiazolylthio)phthalimide is one reactant, there is obtained benzoyl-2-benzothiazolyl disulfide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04119780
출처 데이터셋uspto-grants-1978_10
ORD IDord-a5361563754f43c99387715370b7a68e
출처 메모uspto-grants-1978_10